Abstract

The circadian clock is accountable for the regulation of internal rhythms in most living organisms. It allows the anticipation of environmental changes during the day and a better adaptation of physiological processes. In mammals the main clock is located in the suprachiasmatic nucleus (SCN) and synchronizes secondary clocks throughout the body. Its molecular constituents form an intracellular network which dictates circadian time and regulates clock-controlled genes. These clock-controlled genes are involved in crucial biological processes including metabolism and cell cycle regulation. Its malfunction can lead to disruption of biological rhythms and cause severe damage to the organism. The detailed mechanisms that govern the circadian system are not yet completely understood. Mathematical models can be of great help to exploit the mechanism of the circadian circuitry. We built a mathematical model for the core clock system using available data on phases and amplitudes of clock components obtained from an extensive literature search. This model was used to answer complex questions for example: how does the degradation rate of Per affect the period of the system and what is the role of the ROR/Bmal/REV-ERB (RBR) loop? Our findings indicate that an increase in the RNA degradation rate of the clock gene Period (Per) can contribute to increase or decrease of the period - a consequence of a non-monotonic effect of Per transcript stability on the circadian period identified by our model. Furthermore, we provide theoretical evidence for a potential role of the RBR loop as an independent oscillator. We carried out overexpression experiments on members of the RBR loop which lead to loss of oscillations consistent with our predictions. These findings challenge the role of the RBR loop as a merely auxiliary loop and might change our view of the clock molecular circuitry and of the function of the nuclear receptors (REV-ERB and ROR) as a putative driving force of molecular oscillations.

Highlights

  • Circadian rhythms can be found in most organisms, from bacteria to humans and are a fundamental property of living cells [1]

  • A large number of clock-controlled genes pass on time messages and control several biological processes

  • Characterisation of the gene network – Model design We developed a model for the mammalian circadian clock, which allows the study of the two main feedback loops: ROR/ Bmal/REV-ERB (RBR) and PER/CRY loop (PC)

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Summary

Introduction

Circadian rhythms can be found in most organisms, from bacteria to humans and are a fundamental property of living cells [1]. In mammals the main oscillator resides within the suprachiasmatic nucleus (SCN) and is directly entrained by light via the retinohypothalamic tract [8]. This central pacemaker in the SCN is formed by a set of roughly 20.000 neurons which produce rhythmic outputs and orchestrate local clocks in the brain and peripheral clocks throughout the body. Peripheral clocks in the liver, heart, kidney and skin are implicated in the regulation of local transcriptional activity These can be synchronized by external cues such as temperature and feeding schedules [9,10]

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